
Bulletin of the Chemical Society of Japan p. 1193 - 1200 (1998)
Update date:2022-08-04
Topics:
Murai, Toshiaki
Ezaka, Tatsuya
Kato, Shinzi
The reaction of lithium alkyneselenolates generated from terminal acetylenes, butyllithium, and selenium with amines and allylic bromides proceeded smoothly in THF at 67°C to give 4-penteneselenoamides in moderate to high yields. The reaction may proceed via selenoketene intermediates bearing an allylic group, followed by the attack of amines to give the products. Aliphatic and aromatic acetylenes, silylacetylene, and enynes were employed as terminal acetylenes. One molar amount of secondary amines was effective, whereas an excess of primary amines was necessary. The reactions with 2-hulenyl bromide exhibited high regioselectivity, although they gave the stereoisomeric mixtures. The reactions of silyl ethers of propargylic alcohols gave α,β-unsaturated selenoamides as a product.
View MoreContact:86-25-58619180
Address:Nanjing High-Tech Zone 10 Xinghuo Road Pukou District Nanjing, Jiangsu 210061 The People's Republic of China
Shanghai agrotree chemical co.,ltd.
Contact:+86-21-50117563
Address:Room 8A,liangfeng building,No.8 dongfang RD.pudong,shanghai,China
Shanghai AoBo Bio-Pharmaceutical Technology Co., Ltd.
Contact:+86-21-51320130-801, 816
Address:Room 601, No. 1011, Halei Road, Zhangjiang High-Tech Park, Pudong, Shanghai
qingdao goldenchem imp and exp co.,ltd.
Contact:532-55579246
Address:no.62 ,haier road laoshan distirct
Nanjing Chemzam Pharmtech Co., Ltd.
Contact:+86-25-86462165,+86-13915979898
Address:C5-1,6 Maiyue Road,Maigaoqiao,Nanjing,Jiangsu,China
Doi:10.1021/om9603326
(1996)Doi:10.1016/0277-5387(96)00133-7
(1996)Doi:10.1016/0277-5387(96)00147-7
(1996)Doi:10.1021/jo960830o
(1996)Doi:10.1021/jm00334a035
(1964)Doi:10.1021/om9604583
(1996)